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Volumn 10, Issue 11, 2008, Pages 2143-2145

Asymmetric total synthesis of antiochic acid

Author keywords

[No Author keywords available]

Indexed keywords

ANTIOCHIC ACID; DITERPENE; POLYENE;

EID: 52649140083     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800499p     Document Type: Article
Times cited : (22)

References (34)
  • 1
    • 0019436333 scopus 로고    scopus 로고
    • Isolation and microbiological transformations of related analogues: Ulubelen, A.; Miski, M.; Mabry, T. J. J. Nat. Prod 1981, 44, 119.
    • Isolation and microbiological transformations of related analogues: Ulubelen, A.; Miski, M.; Mabry, T. J. J. Nat. Prod 1981, 44, 119.
  • 5
    • 0005082291 scopus 로고    scopus 로고
    • Previous syntheses of dehydroabietic acid and its analogues: (a) Stork, G.; Schulenberg, J. W. J. Org. Chem. 1962, 84, 284-292.
    • Previous syntheses of dehydroabietic acid and its analogues: (a) Stork, G.; Schulenberg, J. W. J. Org. Chem. 1962, 84, 284-292.
  • 9
    • 33847218271 scopus 로고    scopus 로고
    • Recent progress in total synthesis using polyene cyclization strategy: Sakakura, A.; Ukai, A.; Ishihara, K. Nature 2007, 445, 900-903.
    • Recent progress in total synthesis using polyene cyclization strategy: Sakakura, A.; Ukai, A.; Ishihara, K. Nature 2007, 445, 900-903.
  • 12
    • 33845984909 scopus 로고    scopus 로고
    • and early references cited therein
    • (d) Uyanik, M.; Ishihara, K.; Yamamoto, H. Org. Lett. 2006, 8, 5649-5652, and early references cited therein.
    • (2006) Org. Lett , vol.8 , pp. 5649-5652
    • Uyanik, M.1    Ishihara, K.2    Yamamoto, H.3
  • 15
    • 0029902231 scopus 로고    scopus 로고
    • Corey, E. J., Jr. J. Am. Chem. Soc. 1996, 118, 11982-11983, and references therein.
    • (g) Corey, E. J., Jr. J. Am. Chem. Soc. 1996, 118, 11982-11983, and references therein.
  • 16
  • 27
    • 59849090027 scopus 로고    scopus 로고
    • Polyene 6 was synthesized over seven steps as shown below: (Chemical Equation Presented)
    • Polyene 6 was synthesized over seven steps as shown below: (Chemical Equation Presented)
  • 28
    • 59849084007 scopus 로고    scopus 로고
    • Compound 7 was confirmed to be the THF formation product of 8. The formation yield of 7 was moderate partially because the minor isomer 20 was resistant to cyclization condition and could be recovered. (Chemical Equation Presented)
    • Compound 7 was confirmed to be the THF formation product of 8. The formation yield of 7 was moderate partially because the minor isomer 20 was resistant to cyclization condition and could be recovered. (Chemical Equation Presented)
  • 30
    • 59849091098 scopus 로고    scopus 로고
    • The enantiomeric excess value of 4 was determined on the basis of compound 17 as shown below: (Chemical Equation Presented)
    • The enantiomeric excess value of 4 was determined on the basis of compound 17 as shown below: (Chemical Equation Presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.